Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Omar F. Luna"'
Autor:
Omar F. Luna, Yomkippur V. Perez, Daniele P. Ferrari, Sana S. Sayedipour, Miriam Royo, Gerardo A. Acosta, Luis J. Cruz, Frauke Alves, Erik Agner, Magne O. Sydnes, Fernando Albericio
Publikováno v:
ACS Omega, Vol 9, Iss 32, Pp 34544-34554 (2024)
Externí odkaz:
https://doaj.org/article/a9c3cf5149c04adc9dd0a7f27bf09808
Autor:
Omar F. Luna, Johana Gomez, Constanza Cárdenas, Fernando Albericio, Sergio H. Marshall, Fanny Guzmán
Publikováno v:
Molecules, Vol 21, Iss 11, p 1542 (2016)
The deprotection step is crucial in order to secure a good quality product in Fmoc solid phase peptide synthesis. 9-Fluorenylmethoxycarbonyl (Fmoc) removal is achieved by a two-step mechanism reaction favored by the use of cyclic secondary amines; ho
Externí odkaz:
https://doaj.org/article/f67e144ef06748e98636a56357b7d898
Autor:
Fanny Guzmán, Constanza Cárdenas, Tanya Román, Fernando Albericio, Adriana Gauna, Omar F. Luna, Claudio Alvarez
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Several factors have influenced the increasing presence of peptides as an important class of Active Pharmaceutical Ingredients. One is the continued development of synthetic methodologies for peptide synthesis. Herein, we investigated the Fmoc remova
Publikováno v:
Developmental & Comparative Immunology. 62:48-57
During the early developmental stage of salmonids, high mortality occurs largely as a result of pathogens. These cause low immune competence in fry, producing disease, decreasing production and finally leading to economic losses. Therefore, the aim o
Autor:
Constanza Cárdenas, Paula A. Santana, Claudio Alvarez, Fanny Guzmán, Omar F. Luna, María Soledad Romero, Fernando Albericio
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 23; Issue 4; Pages: 952
Molecules, Vol 23, Iss 4, p 952 (2018)
Molecules; Volume 23; Issue 4; Pages: 952
Molecules, Vol 23, Iss 4, p 952 (2018)
Cyclotides are circular peptides found in various plant families. A cyclized backbone, together with multiple disulfide bonds, confers the peptides’ exceptional stability against protease digestion and thermal denaturation. In addition, the feature
Autor:
Sergio H. Marshall, Fanny Guzmán, Omar F. Luna, Constanza Cárdenas, Johana Gómez, Fernando Albericio
Publikováno v:
Molecules, Vol 21, Iss 11, p 1542 (2016)
Molecules; Volume 21; Issue 11; Pages: 1542
Molecules
Dipòsit Digital de la UB
Universidad de Barcelona
Molecules; Volume 21; Issue 11; Pages: 1542
Molecules
Dipòsit Digital de la UB
Universidad de Barcelona
The deprotection step is crucial in order to secure a good quality product in Fmoc solid phase peptide synthesis. 9-Fluorenylmethoxycarbonyl (Fmoc) removal is achieved by a two-step mechanism reaction favored by the use of cyclic secondary amines; ho